Adenosine Dual Source Computed Tomography (CT) Versus Adenosine Single Photon Emission Computed Tomography (SPECT)
Completed
Conditions studied: Coronary Artery Disease
In brief
Researchers hope that this new non-invasive multi-detector scanner (DSCT) will provide diagnostic information comparable to the combination of traditional SPECT (for function and blood flow) and CT imaging (for a precise anatomical view).
Key facts
- Study ID
- NCT00892307
- Run by
- Cedars-Sinai Medical Center
- People needed
- 34
- Starts
- 2007-02-01
- Expected to finish
- 2011-05-01
- Last updated by the study team
- 2013-11-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Provide written consent and are willing to comply with protocol requirements
- Are at least 18 years of age
- Are referred for clinically-ordered SPECT
- Have known CAD
You may not qualify if…
- Patients being referred to invasive coronary angiography will not be included in this pilot
- Caffeine intake within the 24 hours prior to adenosine stress testing
- Pregnancy (known or suspected)
- Intolerance or contraindication to adenosine (severe Asthma…)
- Intake of methylxanthine containing medications such as theophylline that have not been withdrawn and would interfere with the effectiveness of adenosine.
- Unstable coronary syndromes
- Uncontrolled congestive cardiac failure or cardiogenic shock
- Uncontrolled hypertension with resting BP > 200/110
- More than 30 days between the Adeno-SPECT and the Adeno-DSCT
- Revascularization (percutaneous coronary intervention or coronary artery bypass graft surgery) between the Adeno-SPECT and the Adeno-DSCT
- Change in clinical status as determined by the investigator
- Inability to be on same medication regime 24 hrs prior to Adeno-SPECT and Adeno DSCT
- Patients with chronic renal failure (C.C.T. < 60 ml/m2/sec)
- Patients with allergy to contrast iodinated media
- Congestive heart failure
- History of thromboembolic disorders
- Multiple myeloma
- Hyperthyroidism
- Pheochromocytoma
- Atrial fibrillation
- Inability to perform breath hold for 12 seconds
- Pilot 2:
- All inclusions/exclusions are the same as Pilot 1, WITH THE ADDITION OF:
- Inclusion Criteria:
- Have had prior (within 30 days) positive Adeno-SPECT scan
Where it is running
- Cedars-Sinai Medical Center — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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